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    • 51. 发明申请
    • Method for Making Porous Acicular Mullite-Containing Composites
    • 制备多孔针状莫来石复合材料的方法
    • US20110166018A1
    • 2011-07-07
    • US13059990
    • 2009-09-18
    • Daniel GroholChan HanAleksander J. Pyzik
    • Daniel GroholChan HanAleksander J. Pyzik
    • B01J32/00
    • C04B35/195C04B35/185C04B41/5025C04B2235/3463C04B2235/3481
    • Porous composites of mullite and cordierite are formed by firing an acicular mullite body in the presence of a magnesium source and a silicon source. In some variations of the process, the magnesium and silicon sources are present when the acicular mullite body is formed. In other variations, the magnesium source and the silicon source are applied to a previously-formed acicular mullite body. Surprisingly, the composites have coefficients of linear thermal expansion that are intermediate to those of mullite and cordierite alone, and have higher fracture strengths than cordierite at a similar porosity. Some of the cordierite forms at grain boundaries and/or points of intersection between mullite needles, rather than merely coating the needles. The presence of magnesium and silicon sources during acicular mullite formation does not significantly affect the ability to produce a highly porous network of mullite needles.
    • 莫来石和堇青石的多孔复合材料是通过在镁源和硅源的存在下焙烧针状莫来石体形成的。 在该方法的一些变型中,当形成针状莫来石体时,存在镁和硅源。 在其它变型中,将镁源和硅源施加到预先形成的针状莫来石体上。 令人惊奇的是,复合材料的线性热膨胀系数与莫来石和堇青石单体的中间相似,并且具有比类似孔隙率的堇青石更高的断裂强度。 在莫来石针之间的晶界和/或交叉点处的一些堇青石形式,而不仅仅是涂覆针。 在针状莫来石形成过程中镁和硅源的存在并不会显着影响产生莫来石针的高度多孔网络的能力。
    • 58. 发明授权
    • Self-reinforced silicon nitride ceramic of high fracture toughness
    • 自增强氮化硅陶瓷具有高断裂韧性
    • US5160508A
    • 1992-11-03
    • US826315
    • 1992-01-24
    • Aleksander J. PyzikHarold E. RossowDouglas B. SchwarzDonald R. BeamanBarbara M. PyzikWilliam J. Dubensky
    • Aleksander J. PyzikHarold E. RossowDouglas B. SchwarzDonald R. BeamanBarbara M. PyzikWilliam J. Dubensky
    • C04B35/593C04B35/645C04B35/80
    • C04B35/593C04B35/645C04B35/806
    • A process for preparing a self-reinforced silicon nitride ceramic body of high fracture toughness comprising hot-pressing a powder mixture containing silicon nitride, a densification aid such as sodium oxide, a conversion aid such as lanthanum oxide and a compound, such as gallium oxide, which enhances growth of .beta.-silicon nitride whiskers-under conditions such that densification and the in situ formation of .beta.-silicon nitride whiskers having a high aspect ratio occur. A novel silicon nitride ceramic of high fracture toughness and high fracture strength is disclosed comprising a .beta.-silicon nitride crystalline phase wherein at least about 20 volume percent of the phase is in the form of whiskers having an average aspect ratio of at least about 2.5; a glassy second phase containing the densificaton aid, the conversion aid, the compound which enhances growth of .beta.-silicon nitride whiskers, and an amount of silica; and not greater than about 10 weight percent of the total weight as other phases. The glassy phase may also include a minor amount, e.g., up to 5.0 weight percent, based upon total weight of the ceramic, of aluminum nitride or boron nitride. The glassy phase optionally includes an amount of a secondary reinforcing material such as silicon carbide whiskers.
    • 一种制备高断裂韧性的自增强氮化硅陶瓷体的方法,包括热压含有氮化硅的粉末混合物,致密化助剂例如氧化钠,转化助剂如氧化镧和化合物如氧化镓 ,其增强了β-硅氮化物晶须的生长 - 在使得具有高纵横比的β-硅氮化物晶须的致密化和原位形成的条件下。 公开了一种具有高断裂韧性和高断裂强度的新型氮化硅陶瓷,其包括β-氮化硅结晶相,其中该相的至少约20体积百分数为晶须的形式,其平均纵横比为至少约2.5; 含有致密助剂的玻璃质第二相,转化助剂,增强β-硅氮化物晶须生长的化合物和一定量的二氧化硅; 并且不大于作为其它相的总重量的约10重量%。 玻璃相还可以包括少量,例如,基于陶瓷的总重量,至多5.0重量%的氮化铝或氮化硼。 玻璃相任选地包括一定量的第二增强材料,例如碳化硅晶须。
    • 60. 发明授权
    • B4C/Al cermets and method for making same
    • B4C / Al金属陶瓷及其制造方法
    • US5039633A
    • 1991-08-13
    • US407393
    • 1989-09-14
    • Aleksander J. PyzikRobert T. Nilsson
    • Aleksander J. PyzikRobert T. Nilsson
    • B22F3/26C04B35/65C04B41/50C04B41/51C04B41/87C04B41/88C22C1/10C22C29/00C22C29/02C22C29/06
    • C04B41/009C04B35/652C04B41/507C04B41/515C04B41/5155C04B41/87C04B41/88C22C1/1036C22C29/062
    • Reactive ceramic-metal compositions are described that include a ceramic phase of at least 70 percent by volume, 95 percent of theoretical density and a metal phase that retains its chemical reactivity with the ceramic phase after the composition has been fully densified. The composition may be heat treated after densification to form additional ceramic phases in a controllable manner. Preferred ceramic metal compositions wherein the metal and ceramic components retain reactivity after densification include boron carbide ceramic and Al or Mg metals. The process employed in forming said compositions requires first forming a sintered porous body of the ceramic material followed by contacting with the metal component, which may be in chip or solid bar form. The system is then heated to the melting point of the metal and a pressure of at least 200 MPa is employed such that the porous body is filled with metal and the composition is substantially fully densified. Subsequent heating reacts the metal with the ceramic to form additional B-C-metal phases as desired.
    • 描述了活性陶瓷 - 金属组合物,其包括至少70体积%,理论密度的95%的陶瓷相和在组合物完全致密化后保持其与陶瓷相的化学反应性的金属相。 组合物可以在致密化之后进行热处理,以可控的方式形成额外的陶瓷相。 其中金属和陶瓷组分在致密化后保持反应性的优选陶瓷金属组合物包括碳化硼陶瓷和Al或Mg金属。 用于形成所述组合物的方法需要首先形成陶瓷材料的烧结多孔体,然后与金属组分接触,金属组分可以是片状或固体棒形式。 然后将该系统加热到金属的熔点,并且使用至少200MPa的压力,使得多孔体填充金属并且组合物基本上完全致密化。 随后加热使金属与陶瓷反应,形成额外的B-C金属相。